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A dietary commensal microbe enhances antitumor immunity by activating tumor macrophages to sequester iron

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dc.contributor.authorSharma, Garima-
dc.contributor.authorSharma, Amit-
dc.contributor.authorKim, Inhae-
dc.contributor.authorCha, Dong Gon-
dc.contributor.authorKim, Somi-
dc.contributor.authorPark, Eun Seo-
dc.contributor.authorNoh, Jae Gyun-
dc.contributor.authorLee, Juhee-
dc.contributor.authorKu, Ja Hyeon-
dc.contributor.authorChoi, Yoon Ha-
dc.contributor.authorKong, Jungho-
dc.contributor.authorLee, Haena-
dc.contributor.authorKo, Haeun-
dc.contributor.authorLee, Juhun-
dc.contributor.authorNotaro, Anna-
dc.contributor.authorHong, Seol Hee-
dc.contributor.authorRhee, Joon Haeng-
dc.contributor.authorKim, Sang Geon-
dc.contributor.authorDe Castro, Cristina-
dc.contributor.authorMolinaro, Antonio-
dc.contributor.authorShin, Kunyoo-
dc.contributor.authorKim, Sanguk-
dc.contributor.authorKim, Jong Kyoung-
dc.contributor.authorRudra, Dipayan-
dc.contributor.authorIm, Sin-Hyeog-
dc.date.accessioned2024-08-08T12:31:44Z-
dc.date.available2024-08-08T12:31:44Z-
dc.date.issued2024-05-
dc.identifier.issn1529-2908-
dc.identifier.issn1529-2916-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/22207-
dc.description.abstractInnate immune cells generate a multifaceted antitumor immune response, including the conservation of essential nutrients such as iron. These cells can be modulated by commensal bacteria; however, identifying and understanding how this occurs is a challenge. Here we show that the food commensal Lactiplantibacillus plantarum IMB19 augments antitumor immunity in syngeneic and xenograft mouse tumor models. Its capsular heteropolysaccharide is the major effector molecule, functioning as a ligand for TLR2. In a two-pronged manner, it skews tumor-associated macrophages to a classically active phenotype, leading to generation of a sustained CD8+ T cell response, and triggers macrophage 'nutritional immunity' to deploy the high-affinity iron transporter lipocalin-2 for capturing and sequestering iron in the tumor microenvironment. This process induces a cycle of tumor cell death, epitope expansion and subsequent tumor clearance. Together these data indicate that food commensals might be identified and developed into 'oncobiotics' for a multi-layered approach to cancer therapy. Here the authors show that a heteropolysaccharide from a commensal bacteria commonly found in the Korean food kimchi is able to bolster antitumor immune responses by instructing tumor-associated macrophages to release lipocalin-2, which sequesters iron away from tumor cells contributing to the immune response to attack these cells.-
dc.format.extent12-
dc.language영어-
dc.language.isoENG-
dc.publisherNature Publishing Group-
dc.titleA dietary commensal microbe enhances antitumor immunity by activating tumor macrophages to sequester iron-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1038/s41590-024-01816-x-
dc.identifier.scopusid2-s2.0-85191327803-
dc.identifier.wosid001208246800002-
dc.identifier.bibliographicCitationNature Immunology, v.25, no.5, pp 790 - 801-
dc.citation.titleNature Immunology-
dc.citation.volume25-
dc.citation.number5-
dc.citation.startPage790-
dc.citation.endPage801-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusINNATE IMMUNITY-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusGUT-
dc.subject.keywordPlusHOMEOSTASIS-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordAuthorFerritin-
dc.subject.keywordAuthorGranzyme B-
dc.subject.keywordAuthorInducible Nitric Oxide Synthase-
dc.subject.keywordAuthorInterleukin 2-
dc.subject.keywordAuthorIron-
dc.subject.keywordAuthorPerforin-
dc.subject.keywordAuthorToll Like Receptor 2-
dc.subject.keywordAuthorToll Like Receptor 4-
dc.subject.keywordAuthorIron-
dc.subject.keywordAuthorLipocalin-2-
dc.subject.keywordAuthorToll-like Receptor 2-
dc.subject.keywordAuthorAntineoplastic Agent-
dc.subject.keywordAuthorArginase 1-
dc.subject.keywordAuthorB7 Antigen-
dc.subject.keywordAuthorCd107 Antigen-
dc.subject.keywordAuthorCd11b Antigen-
dc.subject.keywordAuthorCd4 Antigen-
dc.subject.keywordAuthorCd40 Antigen-
dc.subject.keywordAuthorCd8 Antigen-
dc.subject.keywordAuthorCd86 Antigen-
dc.subject.keywordAuthorChemokine Receptor Cx3cr1-
dc.subject.keywordAuthorEpitope-
dc.subject.keywordAuthorFerritin-
dc.subject.keywordAuthorFerroportin-
dc.subject.keywordAuthorGranzyme B-
dc.subject.keywordAuthorHermes Antigen-
dc.subject.keywordAuthorImmune Checkpoint Inhibitor-
dc.subject.keywordAuthorInducible Nitric Oxide Synthase-
dc.subject.keywordAuthorInterleukin 10-
dc.subject.keywordAuthorInterleukin 12p35-
dc.subject.keywordAuthorInterleukin 2-
dc.subject.keywordAuthorIron-
dc.subject.keywordAuthorKlrd1 Protein-
dc.subject.keywordAuthorKlrk1 Protein-
dc.subject.keywordAuthorLactiplantibacillus Plantarum Imb19-
dc.subject.keywordAuthorLigand-
dc.subject.keywordAuthorMajor Histocompatibility Antigen Class 1-
dc.subject.keywordAuthorNeutrophil Gelatinase Associated Lipocalin-
dc.subject.keywordAuthorPerforin-
dc.subject.keywordAuthorPolysaccharide-
dc.subject.keywordAuthorPrf1 Protein-
dc.subject.keywordAuthorProbiotic Agent-
dc.subject.keywordAuthorProgrammed Death 1 Ligand 1-
dc.subject.keywordAuthorProgrammed Death 1 Ligand 1 Antibody-
dc.subject.keywordAuthorRhamnose Rich Heteropolysaccharide-
dc.subject.keywordAuthorRna 16s-
dc.subject.keywordAuthorToll Like Receptor 2-
dc.subject.keywordAuthorToll Like Receptor 4-
dc.subject.keywordAuthorTranscription Factor Foxp3-
dc.subject.keywordAuthorTumor Necrosis Factor-
dc.subject.keywordAuthorUnclassified Drug-
dc.subject.keywordAuthorAnimal Cell-
dc.subject.keywordAuthorAnimal Experiment-
dc.subject.keywordAuthorAnimal Model-
dc.subject.keywordAuthorAnimal Tissue-
dc.subject.keywordAuthorAntineoplastic Activity-
dc.subject.keywordAuthorArticle-
dc.subject.keywordAuthorB16-bl6 Cell Line-
dc.subject.keywordAuthorBinding Affinity-
dc.subject.keywordAuthorCancer Inhibition-
dc.subject.keywordAuthorCancer Therapy-
dc.subject.keywordAuthorCd8+ T Lymphocyte-
dc.subject.keywordAuthorCell Death-
dc.subject.keywordAuthorCommensal-
dc.subject.keywordAuthorControlled Study-
dc.subject.keywordAuthorFeeding Behavior-
dc.subject.keywordAuthorFood Intake-
dc.subject.keywordAuthorHuman-
dc.subject.keywordAuthorHuman Cell-
dc.subject.keywordAuthorImmune Response-
dc.subject.keywordAuthorIron Transport-
dc.subject.keywordAuthorLactiplantibacillus Plantarum-
dc.subject.keywordAuthorLactobacillus-
dc.subject.keywordAuthorMacrophage Activation-
dc.subject.keywordAuthorMetagenomics-
dc.subject.keywordAuthorMouse-
dc.subject.keywordAuthorNonhuman-
dc.subject.keywordAuthorPhenotypic Variation-
dc.subject.keywordAuthorPopulation-
dc.subject.keywordAuthorTumor Associated Leukocyte-
dc.subject.keywordAuthorTumor Cell-
dc.subject.keywordAuthorTumor Growth-
dc.subject.keywordAuthorTumor Immunity-
dc.subject.keywordAuthorTumor Microenvironment-
dc.subject.keywordAuthorTumor Model-
dc.subject.keywordAuthorTumor Xenograft-
dc.subject.keywordAuthorTumor-associated Macrophage-
dc.subject.keywordAuthorAnimal-
dc.subject.keywordAuthorC57bl Mouse-
dc.subject.keywordAuthorFemale-
dc.subject.keywordAuthorImmunology-
dc.subject.keywordAuthorKnockout Mouse-
dc.subject.keywordAuthorMacrophage-
dc.subject.keywordAuthorMetabolism-
dc.subject.keywordAuthorSymbiosis-
dc.subject.keywordAuthorTumor Cell Line-
dc.subject.keywordAuthorAnimals-
dc.subject.keywordAuthorCd8-positive T-lymphocytes-
dc.subject.keywordAuthorCell Line, Tumor-
dc.subject.keywordAuthorFemale-
dc.subject.keywordAuthorHumans-
dc.subject.keywordAuthorIron-
dc.subject.keywordAuthorLipocalin-2-
dc.subject.keywordAuthorMacrophage Activation-
dc.subject.keywordAuthorMacrophages-
dc.subject.keywordAuthorMice-
dc.subject.keywordAuthorMice, Inbred C57bl-
dc.subject.keywordAuthorMice, Knockout-
dc.subject.keywordAuthorSymbiosis-
dc.subject.keywordAuthorToll-like Receptor 2-
dc.subject.keywordAuthorTumor Microenvironment-
dc.subject.keywordAuthorTumor-associated Macrophages-
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